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- source_evidence_literature type ECO_0000212 NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_provenance.
- NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_assertion description "[Linkage to 1p35-p36 (CMT2A), 3q (CMT2B), and 7p (CMT2D) chromosomes has been reported in the disease; however, most HMSN II families do not link to any of the reported loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_provenance.
- NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_assertion evidence source_evidence_literature NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_provenance.
- NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_assertion SIO_000772 9595994 NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_provenance.
- NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_assertion wasDerivedFrom befree-20150227 NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_provenance.
- NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_assertion wasGeneratedBy ECO_0000203 NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP868134.RAavn8pq9S5ekrT-csIiQM-0bhQ6Mk7d7oy1hHn2TGSHg130_provenance.