Matches in Nanopublications for { ?s ?p "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 7 of
7
with 100 items per page.
- NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54212.RAG6rA-YZMvsob6pM2Td-GrlS1WyPYghVRFmz_WwNaI7g130_provenance.
- NP780079.RAmC1GDKDxgS0BVD6O-Om-0oT6YzrriLhBc0y6VkIRWz4130_assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780079.RAmC1GDKDxgS0BVD6O-Om-0oT6YzrriLhBc0y6VkIRWz4130_provenance.
- assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP547257.RAVeAYJxNU5UA0jwMFb52c0ZEKTTiueKhpGR1JomEfRGw130_assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547257.RAVeAYJxNU5UA0jwMFb52c0ZEKTTiueKhpGR1JomEfRGw130_provenance.
- NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547253.RAg1xm95zdXJvlbjZam7qquwVKTYjpGUjSZcqZDSCrcR0130_provenance.
- NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_provenance.