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- source_evidence_literature type ECO_0000212 NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_provenance.
- NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_assertion description "[Biallelic mutations in PALB2 cause FA (Fanconi's anaemia) subtype FA-N, a devastating inherited disorder marked by developmental abnormalities, bone marrow failure and childhood cancer susceptibility, whereas monoallelic mutations predispose to breast, ovarian and pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_provenance.
- NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_assertion evidence source_evidence_literature NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_provenance.
- NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_assertion SIO_000772 24870022 NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_provenance.
- NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_assertion wasDerivedFrom befree-20150227 NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_provenance.
- NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_assertion wasGeneratedBy ECO_0000203 NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP945411.RAyJxUKMuw1fSqnQe-Zeb-4stFE5bQOlCJIptTZD9pXI8130_provenance.