Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance.
- NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_assertion description "[Furthermore, four Italians from the mainland with autosomal recessive hypercholesterolaemia were homozygous for ARH1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance.
- NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_assertion evidence source_evidence_literature NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance.
- NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_assertion SIO_000772 11897284 NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance.
- NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_assertion wasDerivedFrom befree-20140225 NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance.
- NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_assertion wasGeneratedBy ECO_0000203 NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP241208.RAb1oFuJk3I2q5WRTMsmTUF3xGr-DMs2FkxfptNwVX4Fw130_provenance.