Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance.
- NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_assertion description "[Germline inactivating mutations of the CDKN2A gene are the most common cause of inherited susceptibility to melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance.
- NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_assertion evidence source_evidence_literature NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance.
- NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_assertion SIO_000772 16759158 NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance.
- NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_assertion wasDerivedFrom befree-2016 NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance.
- NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_assertion wasGeneratedBy ECO_0000203 NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance.
- befree-2016 importedOn "2016-02-19" NP553464.RAZf5OgL2mM0fbtebiNE0g8U6v_Bj7KaTP7TMx0j7x2vk130_provenance.