Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance.
- NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_assertion description "[These biallelic RTEL1 mutations are responsible for a major subgroup (?29%) of HHS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance.
- NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_assertion evidence source_evidence_literature NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance.
- NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_assertion SIO_000772 23453664 NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance.
- NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_assertion wasDerivedFrom befree-20150227 NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance.
- NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_assertion wasGeneratedBy ECO_0000203 NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP908446.RAcJS5p8R1HL_1idPz9tp0g9zu297i5g8k13ZsX5z-hoQ130_provenance.